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Muscle & Nerve|December 16, 2017
Trajectories of impairment in amyotrophic lateral sclerosis: Insights from the Pooled Resource Open-Access ALS Clinical Trials cohortNimish J Thakore, Brittany R Lapin, Erik P Pioro, et al.Muscle & Nerve|May 19, 2022
Utility of the ALSFRS-R for predicting ALS and comorbid disease neuropathology: The Veterans Affairs Biorepository Brain BankLeigh E Colvin, Zachariah W Foster, Thor D Stein, et al.Muscle & Nerve|January 1, 1987
Creatine kinase isoforms following isometric exerciseP M Clarkson, F S Apple, W C Byrnes, et al.Muscle & Nerve|January 1, 1987
Morphometric studies of sural nerve in childhoodR A Ouvrier, J G McLeod, T ConchinMuscle & Nerve|January 1, 1987
Calmodulin levels in developing muscle tissues and primary cultures of normal and dystrophic (UM-X7.1) hamstersH J Klamut, J A Kotarba, K P StricklandMuscle & Nerve|March 1, 1987
The time course of creatine kinase elevation following concentric needle EMGR Levin, R M Pascuzzi, D E Bruns, et al.Muscle & Nerve|March 1, 1987
Demyelination in vivo by Guillain-Barré syndrome and other human serumM J Brown, J L Rosen, R P LisakMuscle & Nerve|May 26, 2022
A novel method to measure sensory nerve conduction of the posterior antebrachial cutaneous nerveShoji Hemmi, Katsumi Kurokawa, Taiji Nagai, et al.Muscle & Nerve|July 1, 2021
Expert recommendations and clinical considerations in the use of onasemnogene abeparvovec gene therapy for spinal muscular atrophyElizabeth A Kichula, Crystal M Proud, Michelle A Farrar, et al.Muscle & Nerve|June 2, 2021
Relative effects of forced vital capacity and ALSFRS-R on survival in ALSSalah A Daghlas, Raghav Govindarajan, Pageof 898